Variant DetailsVariant: essv15086Internal ID | 9612654 | Landmark | | Location Information | | Cytoband | 17q21.2 | Allele length | Assembly | Allele length | hg38 | 281544 | hg19 | 281544 | hg18 | 281544 | hg17 | 281544 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2758455 | Supporting Variants | | Samples | NA19129 | Known Genes | EIF1, GAST, KRT13, KRT14, KRT15, KRT16, KRT17, KRT19, KRT32, KRT35, KRT36, KRT38, KRT42P, KRT9, LINC00974, MIR6510 | Method | BAC aCGH | Analysis | Array images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd). | Platform | Agilent | Comments | | Reference | Redon_et_al_2006 | Pubmed ID | 17122850 | Accession Number(s) | essv15086
| Frequency | Sample Size | 270 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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